Gene Gene information from NCBI Gene database.
Entrez ID 23109
Gene name Dendrin
Gene symbol DDN
Synonyms (NCBI Gene)
-
Chromosome 12
Chromosome location 12q13.12
miRNA miRNA information provided by mirtarbase database.
121
miRTarBase ID miRNA Experiments Reference
MIRT018142 hsa-miR-335-5p Microarray 18185580
MIRT051128 hsa-miR-16-5p CLASH 23622248
MIRT478339 hsa-miR-24-3p PAR-CLIP 23592263
MIRT478338 hsa-miR-6884-5p PAR-CLIP 23592263
MIRT478337 hsa-miR-485-5p PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IEA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IEA
GO:0005515 Function Protein binding IPI 16464232, 16751601
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IDA 16464232
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610588 24458 ENSG00000181418
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O94850
Protein name Dendrin
Protein function Promotes apoptosis of kidney glomerular podocytes. Podocytes are highly specialized cells essential to the ultrafiltration of blood, resulting in the extraction of urine and the retention of protein (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15498 Dendrin 55 709 Nephrin and CD2AP-binding protein, Dendrin Family
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in brain and kidney. Expressed in kidney glomerular capillary loops (at protein level). {ECO:0000269|PubMed:17251388, ECO:0000269|PubMed:18356187}.
Sequence
Sequence length 711
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BONE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Atrophy Atrophy Pubtator 30458823 Inhibit
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder GWASCAT_DG 27329760
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Focal glomerulosclerosis Glomerulosclerosis BEFREE 30458823
★☆☆☆☆
Found in Text Mining only
IGA Glomerulonephritis Glomerulonephritis BEFREE 30458823
★☆☆☆☆
Found in Text Mining only
Kidney Diseases Kidney Disease BEFREE 17537921
★☆☆☆☆
Found in Text Mining only
Kidney Diseases Kidney disease Pubtator 23667252, 30458823 Associate
★☆☆☆☆
Found in Text Mining only
Lipoid nephrosis Lipoid Nephrosis BEFREE 30458823
★☆☆☆☆
Found in Text Mining only
Macular dystrophy, corneal type 1 Macular corneal dystrophy BEFREE 30458823
★☆☆☆☆
Found in Text Mining only
Nephrotic Syndrome Nephrotic Syndrome LHGDN 18356187
★☆☆☆☆
Found in Text Mining only
Nephrotic Syndrome, Minimal Change Nephrotic Syndrome BEFREE 18356187
★☆☆☆☆
Found in Text Mining only